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Index of reports
> Cases resulting in hospitalization (196)
> Cases with Blood Creatinine Increased (24)
Below is the selection of adverse event reports related to Voltaren (Diclofenac) that includes cases resulting in hospitalization where reactions include blood creatinine increased.
Adverse event in 85 year old female receiving Voltaren (Diclofenac)
Reported by a individual with unspecified qualification from Norway on 2007-10-29
Patient: 85 year old female
Adverse reactions / side effects: Tachycardia, Tricuspid Valve Incompetence, C-Reactive Protein Increased, Dyspepsia, Blood Creatinine Increased, White Blood Cell Count Increased, Anuria, Hiatus Hernia, Diastolic Dysfunction, Renal Cyst, Computerised Tomogram Abnormal, Organ Failure, Haemoglobin Decreased, Hepatic Cyst, Cardiac Failure, Mitral Valve Incompetence, Ejection Fraction Decreased, Peptic Ulcer Perforation
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Ibux
Indication: Myalgia
Prednisolone
Dosage: 10 mg/day
Indication: Myalgia
Voltaren
Indication: Myalgia
Other drugs received by patient: Zantac
Adverse event in 79 year old female receiving Voltaren (Diclofenac)
Reported by a individual with unspecified qualification from France on 2007-10-23
Patient: 79 year old female
Adverse reactions / side effects: Confusional State, Vomiting, Blood Urea Increased, Nausea, Hypotension, Hypoglycaemia, Somnolence, Blood Creatinine Increased, Renal Failure Acute
Adverse event resulted in: hospitalization
Suspect drug(s):
Voltaren
Dosage: 75 mg/day
Administration route: Oral
Indication: Pain
End date: 2007-07-18
Actiskenan
Dosage: 10 mg/day
Administration route: Oral
Indication: Skin Ulcer
Start date: 2007-07-17
End date: 2007-07-18
Zofenil
Dosage: 30 mg/day
Administration route: Oral
Indication: Hypertension
Start date: 2006-11-01
End date: 2007-07-18
Amaryl
Dosage: 1 mg/day
Administration route: Oral
Indication: Type 2 Diabetes Mellitus
Start date: 2006-11-01
End date: 2007-07-18
Lasix
Administration route: Oral
Other drugs received by patient: Levothyrox; Ginkor; Pyostacine; Acetaminophen; Forlax; Diffu K; Vitamin B-12; Sterogyl; Rivotril; Topalgic
Adverse event in 94 year old female receiving Voltaren (Diclofenac)
Reported by a health professional (non-physician/pharmacist) from Italy on 2007-10-16
Patient: 94 year old female
Adverse reactions / side effects: Renal Failure, Blood Potassium Increased, Bundle Branch Block Left, Blood Creatinine Increased
Adverse event resulted in: hospitalization
Suspect drug(s):
Monuril(fosfomycin Trometamol)
Dosage: 3 g po
Administration route: Oral
End date: 2007-07-02
Irbesartan
Dosage: 150 mg po
Administration route: Oral
Preterax
End date: 2007-07-02
Iperten(manidipne Hydrochloride)
Temerit (Nebivolol)
Lasix
Dosage: 20 mg
Mediatensyl (Urapidil)
Discortrine (Glyceryl Trinitrate)
Plavix
Vastarel (Trimetazidine)
Dosage: 35 mg qd po
Administration route: Oral
End date: 2007-07-02
Pantoprazole Sodium
Dosage: 20 mg po
Administration route: Oral
End date: 2007-07-02
DI-Antalvic
End date: 2007-07-02
Lansoyl (Parrafin, Liquid)
End date: 2007-07-02
Voltaren
Fenofibrate
Duragesic-100
Motilyo (Domperidone)
Acarbose
Bactrim DS
End date: 2007-07-02
Flector EP Gel (Diclofenac Epolaminum)
Dafalgan Codeine
Adverse event in male receiving Voltaren (Diclofenac)
Reported by a individual with unspecified qualification from Japan on 2007-10-12
Patient: male
Adverse reactions / side effects: Blood Urea Increased, Hyperkalaemia, Hypoglycaemia, Hyponatraemia, Acidosis, C-Reactive Protein Increased, Sepsis, Dehydration, Adrenal Insufficiency, Enteritis Infectious, Blood Creatinine Increased, Shock, Renal Failure Acute, Anuria
Adverse event resulted in: hospitalization
Suspect drug(s):
Voltaren (Diclofenac)
Adverse event in 61 year old female receiving Voltaren (Diclofenac)
Reported by a individual with unspecified qualification from Japan on 2007-07-16
Patient: 61 year old female, weighing 59.0 kg (129.8 pounds)
Adverse reactions / side effects: Blood Bilirubin Increased, Drug Eruption, Thoracic Cavity Drainage, Disseminated Intravascular Coagulation, Pyrexia, Erythema, Laboratory Test Abnormal, Gamma-Glutamyltransferase Increased, C-Reactive Protein Increased, Pleural Effusion, Blood Creatinine Increased, Lymphocyte Count Decreased, Oxygen Saturation Decreased, White Blood Cell Count Increased, Blood Urea Increased, Dyspnoea, Neutrophil Count Increased, Monocyte Count Decreased, Alanine Aminotransferase Increased, Blood Lactate Dehydrogenase Increased, Urine Output Decreased, Lymphocyte Stimulation Test Positive, Rash Macular, Haemoglobin Decreased, Renal Failure, Aspartate Aminotransferase Increased, Oliguria, Platelet Count Decreased, Lung Infiltration
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Voltaren
Dosage: 37.5 mg/day
Administration route: Oral
Indication: Pyrexia
Start date: 2005-11-09
End date: 2005-11-10
Loxonin
Dosage: 60 mg, tid
Administration route: Oral
Indication: Pyrexia
Start date: 2005-11-10
End date: 2005-11-13
Dacarbazine
Dosage: 180 mg/day
Indication: Malignant Melanoma
Start date: 2005-11-08
End date: 2005-11-12
Nidran
Dosage: 100 mg/day
Indication: Malignant Melanoma
Start date: 2005-11-08
End date: 2005-11-08
Oncovin
Dosage: 1 mg/day
Indication: Malignant Melanoma
Start date: 2005-11-08
End date: 2005-11-08
Feron
Dosage: 3000000 iu/day
Indication: Malignant Melanoma
Start date: 2005-11-08
End date: 2005-11-12
Other drugs received by patient: Norvasc; Towamin; Lipitor; Voglibose
Adverse event in 20 year old male receiving Voltaren (Diclofenac)
Reported by a health professional (non-physician/pharmacist) from Japan on 2007-07-16
Patient: 20 year old male, weighing 55.0 kg (121.0 pounds)
Adverse reactions / side effects: Blood Bilirubin Increased, Drug Eruption, Disseminated Intravascular Coagulation, Pyrexia, Haematocrit Decreased, RED Blood Cell Count Decreased, Gamma-Glutamyltransferase Increased, Dermatitis Bullous, Blood Creatinine Increased, Melaena, Blister, Stevens-Johnson Syndrome, White Blood Cell Count Increased, Blood Pressure Increased, Pneumonia, Histiocytosis Haematophagic, Blood Urea Increased, Alanine Aminotransferase Increased, Life Support, Pulmonary Haemorrhage, Mucosal Erosion, Haemoglobin Decreased, Aspartate Aminotransferase Increased, Platelet Count Decreased, Skin Erosion
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Voltaren
Dosage: unk, unk
Administration route: Oral
Indication: Pyrexia
Voltaren
Dosage: 25 mg/day
Start date: 2007-03-22
End date: 2007-03-29
Loxoprofen
Dosage: 60 mg/day
Administration route: Oral
Indication: Headache
Start date: 2007-03-28
End date: 2007-04-03
Meropen
Dosage: 1.5 g/day
Indication: Infection
Start date: 2007-03-23
End date: 2007-03-28
Other drugs received by patient: Minocycline HCL; Rocephin; Zyvox; Amikacin; Funguard
Adverse event in 20 year old male receiving Voltaren (Diclofenac)
Reported by a health professional (non-physician/pharmacist) from Japan on 2007-07-16
Patient: 20 year old male, weighing 55.0 kg (121.0 pounds)
Adverse reactions / side effects: Blood Bilirubin Increased, Drug Eruption, Disseminated Intravascular Coagulation, Pyrexia, Haematocrit Decreased, RED Blood Cell Count Decreased, Gamma-Glutamyltransferase Increased, Dermatitis Bullous, Blood Creatinine Increased, Melaena, Blister, Stevens-Johnson Syndrome, White Blood Cell Count Increased, Blood Pressure Increased, Pneumonia, Histiocytosis Haematophagic, Blood Urea Increased, Alanine Aminotransferase Increased, Life Support, Pulmonary Haemorrhage, Mucosal Erosion, Haemoglobin Decreased, Aspartate Aminotransferase Increased, Platelet Count Decreased, Skin Erosion
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Voltaren
Dosage: unk, unk
Administration route: Oral
Indication: Pyrexia
Voltaren
Dosage: 25 mg/day
Start date: 2007-03-22
End date: 2007-03-29
Loxoprofen
Dosage: 60 mg/day
Administration route: Oral
Indication: Headache
Start date: 2007-03-28
End date: 2007-04-03
Meropen
Dosage: 1.5 g/day
Indication: Infection
Start date: 2007-03-23
End date: 2007-03-28
Other drugs received by patient: Minocycline HCL; Rocephin; Zyvox; Amikacin; Funguard
Adverse event in 70 year old female receiving Voltaren (Diclofenac)
Reported by a physician from Japan on 2007-07-13
Patient: 70 year old female, weighing 36.0 kg (79.2 pounds)
Adverse reactions / side effects: Hyperhidrosis, Cardiac Massage, Blood Creatinine Increased, White Blood Cell Count Increased, Metabolic Acidosis, Blood Lactate Dehydrogenase Increased, Hypotension, Urine Output Decreased, Haemodialysis, Respiratory Rate Decreased, Heart Rate Decreased, Aspartate Aminotransferase Increased, Depressed Level of Consciousness, Anaphylactic Shock, Pallor, Haematocrit Decreased, RED Blood Cell Count Decreased, Tachypnoea, Oxygen Supplementation, Hepatitis Fulminant, Oxygen Saturation Decreased, Blood Urea Increased, Mydriasis, Drug Hypersensitivity, Alanine Aminotransferase Increased, Life Support, Hepatic Enzyme Increased, Haemoglobin Decreased, Blood Glucose Decreased, Catheterisation Cardiac, Feeling Abnormal, Electrocardiogram ST Segment Elevation
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Voltaren (Diclofenac)
Other drugs received by patient: Loxonin; Pentagin; Aspirin; Ticlopidine HCL; Sigmart; Lansoprazole; Artist; Ferromia
Adverse event in 70 year old female receiving Voltaren (Diclofenac)
Reported by a physician from Japan on 2007-07-13
Patient: 70 year old female, weighing 36.0 kg (79.2 pounds)
Adverse reactions / side effects: Hyperhidrosis, Cardiac Massage, Blood Creatinine Increased, White Blood Cell Count Increased, Metabolic Acidosis, Urine Output Decreased, Blood Lactate Dehydrogenase Increased, Hypotension, Haemodialysis, Respiratory Rate Decreased, Heart Rate Decreased, Aspartate Aminotransferase Increased, Depressed Level of Consciousness, Intubation, Anaphylactic Shock, Pallor, Haematocrit Decreased, RED Blood Cell Count Decreased, Tachypnoea, Oxygen Supplementation, Hepatitis Fulminant, Oxygen Saturation Decreased, Blood Urea Increased, Mydriasis, Alanine Aminotransferase Increased, Drug Hypersensitivity, Life Support, Hepatic Enzyme Increased, Haemoglobin Decreased, Blood Glucose Decreased, Catheterisation Cardiac, Feeling Abnormal, Electrocardiogram ST Segment Elevation
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Voltaren (Diclofenac)
Other drugs received by patient: Loxonin; Pentagin; Aspirin; Ticlopidine HCL; Sigmart; Lansoprazole; Artist; Ferromia
Adverse event in 17 year old female receiving Voltaren (Diclofenac)
Reported by a physician from Germany on 2007-07-06
Patient: 17 year old female, weighing 45.0 kg (99.0 pounds)
Adverse reactions / side effects: Renal Disorder, Haematuria, Glomerular Filtration Rate Increased, Transaminases Increased, Gamma-Glutamyltransferase Increased, Albuminuria, Flank Pain, Proteinuria, Blood Creatinine Increased
Adverse event resulted in: hospitalization
Suspect drug(s):
Voltaren
Dosage: 75 mg, qd
Administration route: Oral
Indication: Bone Pain
Start date: 2007-05-08
End date: 2007-05-08
Voltaren
Dosage: 150mg/day
Administration route: Oral
Start date: 2007-05-09
End date: 2007-05-09
Adverse event in 11 year old male receiving Voltaren (Diclofenac)
Reported by a individual with unspecified qualification from Japan on 2007-06-07
Patient: 11 year old male, weighing 32.0 kg (70.4 pounds)
Adverse reactions / side effects: Blood PH Increased, Disseminated Intravascular Coagulation, Blood Albumin Decreased, Petechiae, Pyrexia, Erythema, Blood Fibrinogen Decreased, Interstitial Lung Disease, C-Reactive Protein Increased, Acute Respiratory Distress Syndrome, Blood Creatinine Increased, White Blood Cell Count Increased, Cough, Renal Failure Acute, Hypertensive Encephalopathy, Dyspnoea, Blood Urea Increased, Blood Lactate Dehydrogenase Increased, Alanine Aminotransferase Increased, Pancytopenia, Life Support, Rash, Protein Total Decreased, Lymphocyte Stimulation Test Positive, Aspartate Aminotransferase Increased, Platelet Count Decreased, PO2 Increased, Lung Infiltration, Calculus Ureteric
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Voltaren (Diclofenac)
Other drugs received by patient: Predonine; Bufferin; Sulpyrine; Kashilon; Cefazolin Sodium; Methylprednisolone 16mg TAB
Adverse event in 11 year old male receiving Voltaren (Diclofenac)
Reported by a individual with unspecified qualification from Japan on 2007-06-04
Patient: 11 year old male, weighing 32.0 kg (70.4 pounds)
Adverse reactions / side effects: Blood PH Increased, Disseminated Intravascular Coagulation, Petechiae, Blood Albumin Decreased, Blood Fibrinogen Decreased, C-Reactive Protein Increased, Acute Respiratory Distress Syndrome, Blood Creatinine Increased, White Blood Cell Count Increased, Renal Failure Acute, Cough, Dyspnoea, Blood Urea Increased, Alanine Aminotransferase Increased, Blood Lactate Dehydrogenase Increased, Pancytopenia, Protein Total Decreased, Lymphocyte Stimulation Test Positive, Rash, Aspartate Aminotransferase Increased, Platelet Count Decreased, PO2 Increased, Lung Infiltration, Calculus Ureteric
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Voltaren (Diclofenac)
Other drugs received by patient: Predonine; Bufferin; Sulpyrine; Kashilon; Cefazolin Sodium
Adverse event in 41 year old male receiving Voltaren (Diclofenac)
Reported by a physician from Japan on 2007-05-11
Patient: 41 year old male, weighing 60.0 kg (132.0 pounds)
Adverse reactions / side effects: Brain Death, Rhabdomyolysis, Blood Creatine Phosphokinase Increased, Blood Calcium Increased, Pyrexia, C-Reactive Protein Increased, Brain Oedema, Blood Creatinine Increased, White Blood Cell Count Increased, Mydriasis, Brain Stem Haemorrhage, Blood Urea Increased, Dyspnoea, Urine Output Decreased, Alanine Aminotransferase Increased, Blood Lactate Dehydrogenase Increased, Dependence ON Respirator, Haemodialysis, Brain Stem Syndrome, Dehydration, Aspartate Aminotransferase Increased, Platelet Count Decreased, Blood Pressure Decreased
Adverse event resulted in: death, life threatening event, hospitalization
Suspect drug(s):
Voltaren (Diclofenac)
Other drugs received by patient: Adona; Transamin; Primperan INJ; Gaster; Glyceol
Adverse event in 80 year old female receiving Voltaren (Diclofenac)
Reported by a individual with unspecified qualification from France on 2007-04-24
Patient: 80 year old female, weighing 45.0 kg (99.0 pounds)
Adverse reactions / side effects: Confusional State, Blood Creatine Phosphokinase Increased, Creatinine Renal Clearance Decreased, Anaemia, Hyponatraemia, Fall, Blood Calcium Decreased, Blood Potassium Decreased, Dehydration, Carbon Dioxide Decreased, Injury, Blood Creatinine Increased
Adverse event resulted in: hospitalization
Suspect drug(s):
Irbesartan
Dosage: 1 df, qd
Administration route: Oral
Indication: Essential Hypertension
End date: 2006-12-12
Voltaren
Administration route: Oral
End date: 2006-12-12
Other drugs received by patient: Orocal; Kardegic; Stilnox / FRA /; Victan
Adverse event in 80 year old female receiving Voltaren (Diclofenac)
Reported by a individual with unspecified qualification from France on 2007-04-24
Patient: 80 year old female, weighing 45.0 kg (99.0 pounds)
Adverse reactions / side effects: Confusional State, Blood Creatine Phosphokinase Increased, Creatinine Renal Clearance Decreased, Anaemia, Hyponatraemia, Fall, Blood Calcium Decreased, Blood Potassium Decreased, Dehydration, Carbon Dioxide Decreased, Injury, Blood Creatinine Increased
Adverse event resulted in: hospitalization
Suspect drug(s):
Irbesartan
Dosage: 1 df, qd
Administration route: Oral
Indication: Essential Hypertension
End date: 2006-12-12
Voltaren
Administration route: Oral
End date: 2006-12-12
Other drugs received by patient: Orocal; Kardegic; Stilnox / FRA /; Victan
Adverse event in 41 year old male receiving Voltaren (Diclofenac)
Reported by a physician from Japan on 2007-04-06
Patient: 41 year old male, weighing 60.0 kg (132.0 pounds)
Adverse reactions / side effects: Brain Death, Rhabdomyolysis, Blood Creatine Phosphokinase Increased, Blood Calcium Increased, Pyrexia, C-Reactive Protein Increased, Brain Oedema, Blood Creatinine Increased, White Blood Cell Count Increased, Mydriasis, Brain Stem Haemorrhage, Blood Urea Increased, Dyspnoea, Urine Output Decreased, Alanine Aminotransferase Increased, Blood Lactate Dehydrogenase Increased, Dependence ON Respirator, Haemodialysis, Brain Stem Syndrome, Dehydration, Aspartate Aminotransferase Increased, Platelet Count Decreased, Blood Pressure Decreased
Adverse event resulted in: death, life threatening event, hospitalization
Suspect drug(s):
Voltaren (Diclofenac)
Other drugs received by patient: Adona; Transamin; Primperan INJ; Gaster; Glyceol
Adverse event in 81 year old female receiving Voltaren (Diclofenac)
Reported by a individual with unspecified qualification from Italy on 2007-03-28
Patient: 81 year old female
Adverse reactions / side effects: Confusional State, Blood Urea Increased, Balance Disorder, Nausea, Vertigo, Blood Creatinine Increased, Renal Failure Acute
Adverse event resulted in: hospitalization
Suspect drug(s):
Voltaren
Dosage: 100 mg, bid
Administration route: Oral
Indication: Pain
Start date: 2007-02-27
End date: 2007-03-03
Talavir
Dosage: 1 g, tid
Indication: Herpes Zoster
Start date: 2007-02-28
End date: 2007-03-03
Other drugs received by patient: Cardirene; Cotareg; Glucophage; Actos
Adverse event in 81 year old female receiving Voltaren (Diclofenac)
Reported by a individual with unspecified qualification from Italy on 2007-03-26
Patient: 81 year old female
Adverse reactions / side effects: Confusional State, Blood Urea Increased, Balance Disorder, Nausea, Vertigo, Blood Creatinine Increased, Renal Failure Acute
Adverse event resulted in: hospitalization
Suspect drug(s):
Voltaren
Dosage: 100 mg, bid
Administration route: Oral
Indication: Pain
Start date: 2007-02-27
End date: 2007-03-03
Talavir
Dosage: 1 g, tid
Indication: Herpes Zoster
Start date: 2007-02-28
End date: 2007-03-03
Other drugs received by patient: Cardirene; Cotareg; Glucophage; Actos
Adverse event in 91 year old female receiving Voltaren (Diclofenac)
Reported by a health professional (non-physician/pharmacist) from Norway on 2007-03-26
Patient: 91 year old female
Adverse reactions / side effects: Blood Calcium Increased, Drug Interaction, Platelet Count Increased, Constipation, Muscle Rigidity, Gastrointestinal Ulcer, Hypokinesia, C-Reactive Protein Increased, Methylmalonic Aciduria, Bacterial DNA Test Positive, Blood Sodium Decreased, Blood Creatinine Increased, Decreased Appetite, White Blood Cell Count Increased, Blood Iron Decreased, Endoscopy, Thyroxine Increased, Eating Disorder, Haematochezia, Blood Potassium Decreased, Mental Disorder, Tardive Dyskinesia, Alanine Aminotransferase Decreased
Adverse event resulted in: hospitalization
Suspect drug(s):
Voltaren
Administration route: Oral
End date: 2007-02-01
Prednisolone
Dosage: unk, unk
Administration route: Oral
Indication: Myalgia
Start date: 2006-12-01
End date: 2007-02-01
Trilafon
Dosage: 8 mg daily
Administration route: Oral
End date: 2007-02-25
Albyl-E
Dosage: 160 mg daily
Administration route: Oral
Other drugs received by patient: Plendil; Atacand HCT; Selo-ZOK
Adverse event in 41 year old male receiving Voltaren (Diclofenac)
Reported by a physician from Japan on 2007-03-16
Patient: 41 year old male, weighing 60.0 kg (132.0 pounds)
Adverse reactions / side effects: Brain Death, Rhabdomyolysis, Blood Creatine Phosphokinase Increased, Blood Calcium Increased, Pyrexia, C-Reactive Protein Increased, Brain Oedema, Blood Creatinine Increased, White Blood Cell Count Increased, Mydriasis, Brain Stem Haemorrhage, Blood Urea Increased, Dyspnoea, Urine Output Decreased, Alanine Aminotransferase Increased, Blood Lactate Dehydrogenase Increased, Dependence ON Respirator, Haemodialysis, Brain Stem Syndrome, Dehydration, Aspartate Aminotransferase Increased, Platelet Count Decreased, Blood Pressure Decreased
Adverse event resulted in: death, life threatening event, hospitalization
Suspect drug(s):
Voltaren (Diclofenac)
Other drugs received by patient: Adona; Transamin; Primperan INJ; Gaster; Glyceol
Adverse event in 80 year old female receiving Voltaren (Diclofenac)
Reported by a individual with unspecified qualification from France on 2007-03-06
Patient: 80 year old female, weighing 45.0 kg (99.0 pounds)
Adverse reactions / side effects: Confusional State, Blood Creatine Phosphokinase Increased, Creatinine Renal Clearance Decreased, Anaemia, Hyponatraemia, Fall, Blood Calcium Decreased, Blood Potassium Decreased, Dehydration, Carbon Dioxide Decreased, Injury, Blood Creatinine Increased
Adverse event resulted in: hospitalization
Suspect drug(s):
Orocal
Dosage: 1.25 g, qd
Administration route: Oral
Kardegic
Dosage: 1 df, qd
Administration route: Oral
Irbesartan
Dosage: 1 df, qd
Administration route: Oral
Indication: Essential Hypertension
End date: 2006-12-12
Stilnox / FRA /
Dosage: 10 mg, unk
Administration route: Oral
Victan
Dosage: 1 mg, qd
Administration route: Oral
Voltaren
Administration route: Oral
End date: 2006-12-12
Adverse event in 84 year old female receiving Voltaren (Diclofenac)
Reported by a individual with unspecified qualification from France on 2007-02-23
Patient: 84 year old female, weighing 66.0 kg (145.2 pounds)
Adverse reactions / side effects: Hyperkalaemia, Rales, Hypochromasia, Walking AID User, Activated Partial Thromboplastin Time Prolonged, Impaired Self-Care, Blood Creatinine Increased, Renal Failure Acute, Prothrombin Time Ratio Increased, Cataract, Blood Urea Increased, General Physical Health Deterioration, Haemoglobin Decreased, Electrocardiogram T Wave Amplitude Increased, Anxiety, Hallucination, Visual, Charles Bonnet Syndrome, Gait Disturbance, Atrioventricular Block First Degree
Adverse event resulted in: hospitalization
Suspect drug(s):
Voltaren (Diclofenac)
Other drugs received by patient possibly interacting with the suspect drug:
Triatec
Dosage: 5 mg, qd
Administration route: Oral
Indication: Essential Hypertension
End date: 2006-12-21
Other drugs received by patient: Allopurinol Sodium; Inipomp; Acetaminophen; Torental; Furosemide; Efferalgan Codeine; Soprol; Haldol
Adverse event in 84 year old female receiving Voltaren (Diclofenac)
Reported by a individual with unspecified qualification from France on 2007-02-22
Patient: 84 year old female, weighing 66.0 kg (145.2 pounds)
Adverse reactions / side effects: Hyperkalaemia, Rales, Hypochromasia, Walking AID User, Activated Partial Thromboplastin Time Prolonged, Impaired Self-Care, Blood Creatinine Increased, Renal Failure Acute, Prothrombin Time Ratio Increased, Cataract, Blood Urea Increased, General Physical Health Deterioration, Haemoglobin Decreased, Electrocardiogram T Wave Amplitude Increased, Anxiety, Hallucination, Visual, Charles Bonnet Syndrome, Gait Disturbance, Atrioventricular Block First Degree
Adverse event resulted in: hospitalization
Suspect drug(s):
Voltaren (Diclofenac)
Other drugs received by patient possibly interacting with the suspect drug:
Triatec
Dosage: 5 mg, qd
Administration route: Oral
Indication: Essential Hypertension
End date: 2006-12-21
Other drugs received by patient: Allopurinol Sodium; Inipomp; Acetaminophen; Torental; Furosemide; Efferalgan Codeine; Soprol; Haldol
Adverse event in 75 year old female receiving Voltaren (Diclofenac)
Reported by a individual with unspecified qualification from Spain on 2007-02-19
Patient: 75 year old female
Adverse reactions / side effects: Blood Urea Increased, Microlithiasis, Drug Interaction, Blood Creatinine Increased, Blood Fibrinogen Increased, White Blood Cell Count Increased, Renal Failure Acute
Adverse event resulted in: hospitalization
Suspect drug(s):
Voltaren
Ketesse
Dosage: 75 mg/day
Administration route: Oral
Indication: Cellulitis
Start date: 2006-04-15
End date: 2006-04-24
Aspirin
Dosage: 100 mg/day
Administration route: Oral
Plavix
Eneas
Indication: Essential Hypertension
End date: 2006-04-24
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